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Showing papers by "Richard D. Averitt published in 1998"


Journal ArticleDOI
TL;DR: In this paper, a general approach to the making of metal nanoshell composite nanoparticles based on molecular self-assembly and colloid reduction chemistry is described, which can be used to construct a new, composite nanoparticle whose optical resonance can be designed in a controlled manner.

2,240 citations


Journal ArticleDOI
TL;DR: In this paper, the plasmon frequency of these nanoparticles can be controlled by varying the ratio of the core diameter to shell thickness, and the induced change in transmission of gold nanoshell films to the electron dynamics in the thin gold shell.
Abstract: We present ultrafast optical studies on nanoshells, which consist of a nanoscale ${\mathrm{Au}}_{2}\mathrm{S}$ dielectric core surrounded by an ultrathin Au shell. The plasmon frequency of these nanoparticles can be controlled by varying the ratio of the core diameter to shell thickness. By tuning this plasmon peak, we have observed both transient bleaching and transient absorption for Au nanoshells embedded in polyvinyl alcohol. We relate the induced change in transmission of gold nanoshell films to the electron dynamics in the thin gold shell. Our results indicate that even when the plasmon frequency is shifted below the onset of interband transitions, interband effects are still of primary importance in determining the nonlinear optical response. An electron relaxation time of $1.65\ifmmode\pm\else\textpm\fi{}0.10\mathrm{ps}$ is measured that corresponds to an electron-phonon coupling constant of $2.2\ifmmode\times\else\texttimes\fi{}{10}^{16}{\mathrm{W}/(\mathrm{m}}^{3}\mathrm{}\mathrm{K}),$ smaller than that observed in bulk Au films.

107 citations